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Open Versus Robot Assisted Radical Cystectomy With Totally Intracorporeal Urinary Diversion.

Primary Purpose

Bladder Cancer

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Open or robotic radical cystectomy
Sponsored by
Regina Elena Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bladder Cancer focused on measuring Open Radical Cystectomy, Robotic Radical cystectomy, Intracorporeal urinary diversion, Prospective randdomized trial

Eligibility Criteria

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Inclusion Criteria:

  • Patients with muscle invasive high grade urothelial carcinoma (and variant histologies) of the bladder or high grade non muscle invasive BCG recurrent/refractory disease.

Exclusion Criteria:

  • Cystectomy without curative intent (palliative, salvage).
  • Patients unfit for robotic cystectomy.

Sites / Locations

  • Regina Elena NCI

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Open Radical Cystectomy

Robot assisted radical cystectomy

Arm Description

Open Radical Cystectomy, pelvic lymph node dissection, urinary diversion (neobladder or ileal conduit)

Robot assisted radical cystectomy, pelvic lymph node dissection, intracorporeal urinary diversion (neobladder or ileal conduit)

Outcomes

Primary Outcome Measures

Number of participants requiring perioperative transfusions.
50% reduction of perioperative transfusion rates in robotic arm.

Secondary Outcome Measures

Number of participants requiring insertion of nasogastric tube
Comparison between open and robotic arms.
Incidence of Clavien grade 1-2 perioperative complications at 30-d evaluation.
Comparison between open and robotic arms.
Incidence of Clavien grade 1-2 perioperative complications at 90-d evaluation.
Comparison between open and robotic arms.
Incidence of Clavien grade 1-2 perioperative complications at 180-d evaluation.
Comparison between open and robotic arms.
Incidence of patients requiring readmission.
Comparison between open and robotic arms.
Cost analysis.
Comparison between open and robotic arms.

Full Information

First Posted
January 26, 2018
Last Updated
January 18, 2023
Sponsor
Regina Elena Cancer Institute
Collaborators
Ministero della Salute, Italy
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1. Study Identification

Unique Protocol Identification Number
NCT03434132
Brief Title
Open Versus Robot Assisted Radical Cystectomy With Totally Intracorporeal Urinary Diversion.
Official Title
Open Versus Robot Assisted Radical Cystectomy With Totally Intracorporeal Urinary Diversion. Single Centre Prospective Randomized Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
January 29, 2018 (Actual)
Primary Completion Date
October 30, 2020 (Actual)
Study Completion Date
September 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Regina Elena Cancer Institute
Collaborators
Ministero della Salute, Italy

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This prospective randomized study is designed to provide high level of evidence supporting superiority of robot assisted (RA) versus open (O) radical cystectomy (RC). The primary endpoint is a 50% reduction of transfusion rate, several perioperative outcomes potentially linked to a reduced invasiveness are considered as secondary endpoints. Investigators hypothesis is that the reduced invasiveness of RARC might turn into a higher adherence to enhanced recovery after surgery (ERAS) protocols (early bowel recovery, reduced need for painkillers and insertion of nasogastric tube) and consequently to shorter hospital stay and to faster return to daily activities. These data will be taken into account in a matched cost analysis between arms. Secondary aims include a between arm matched comparison of perioperative complications, oncologic outcomes (2-yr disease free survival is an accepted surrogate of long term oncologic effectiveness of RC) and functional outcomes (daytime and nighttime continence).
Detailed Description
Despite encouraging data deriving from colorectal surgery, evidences in favor to ERAS protocols following RARC are poor. Moreover, according to a recent survey of surgeons with a specialist interest in RC, the adherence to ERAS protocols is <20% [1]. Retrospective and preliminary data from the robotic consortium have supported oncologic effectiveness of RARC; however in the only prospective randomized trial comparing RARC and ORC urinary diversions were performed extracorporeally, potentially impairing the benefits of minimally invasive surgery [2]. Robot assisted radical cystectomy (RARC) has the aim of providing adequate cancer control while minimizing invasiveness of open radical cystectomy (ORC). The primary end-point of this trial is to demonstrate a reduction of perioperative transfusion rate in RARC arm by 50% compared to ORC arm. ERAS protocols may significantly contribute to shortening length of hospital stay, a key outcome in this clinical setting of patients receiving RC, being the mean length of hospital stay around 14 days in Italy. Investigators' hypothesis is that the reduced invasiveness of RARC might contribute to an increased adoption of ERAS protocols (reduced need for reinsertion of nasogastric tube, shorter time to first flatus, to mobilization, to regular diet and finally shorter duration of hospital stay). Assessment of oncologic outcomes of RARC, although not the primary endpoint of the present study, is certainly an outcome of interest. The expected duration of enrollment (18 mo) should provide 2-yr oncologic outcomes for about 66% of patients. Two-year recurrence free survival has been reported as a valid surrogate marker of long term oncologic survival after RC. Specific Aim 1:To demonstrate superiority of RARC versus ORC in terms of 50% reduction of perioperative transfusion rates. Specific Aim 2: To evaluate invasiveness of both surgical approaches by assessing the adherence to ERAS protocols in both and the incidence of perioperative and 30-d, 90d, 180d complications, readmission rates (30d, 90d). Cost analysis will assess the potential impact of shorter hospital stay on overall costs of robotic procedures. Specific Aim 3: To assess quality of life at 6-mo, 12-mo and 24-mo follow-up evaluation and to perform a matched comparison of oncologic and functional outcomes between two arms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer
Keywords
Open Radical Cystectomy, Robotic Radical cystectomy, Intracorporeal urinary diversion, Prospective randdomized trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
116 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Open Radical Cystectomy
Arm Type
Active Comparator
Arm Description
Open Radical Cystectomy, pelvic lymph node dissection, urinary diversion (neobladder or ileal conduit)
Arm Title
Robot assisted radical cystectomy
Arm Type
Experimental
Arm Description
Robot assisted radical cystectomy, pelvic lymph node dissection, intracorporeal urinary diversion (neobladder or ileal conduit)
Intervention Type
Procedure
Intervention Name(s)
Open or robotic radical cystectomy
Intervention Description
ORC and orthotopic ileal neobladder is performed as previously described. A separate package PLND is performed as in open as in robotic surgery. RARC is performed replicating open surgical procedure. The orthotopic ileal neobladder model used is the 'vescica ileale padovana' as previously described. An ileal segment, approximately 42 cm long, is chosen at a minimum distance of 20cm far from ileo-cecal valve. A latero-lateral ileal anastomosis is performed with staplers to restore bowel continuity. For ileal conduit, a 20cm ileal segment (approximately 20 cm long) at a minimum distance of 20 cm from ileo-cecal valve is isolated and transected with staplers. Bowel continuity is restored as previously described. The ileal loop on its distal edge is extracted through abdomen wall at the previously identified stoma point and fixed to abdomen fascia. The ureters are spatulated and a latero-lateral anastomosis according to Wallace 1 technique is performed.
Primary Outcome Measure Information:
Title
Number of participants requiring perioperative transfusions.
Description
50% reduction of perioperative transfusion rates in robotic arm.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Number of participants requiring insertion of nasogastric tube
Description
Comparison between open and robotic arms.
Time Frame
30 days
Title
Incidence of Clavien grade 1-2 perioperative complications at 30-d evaluation.
Description
Comparison between open and robotic arms.
Time Frame
30 days
Title
Incidence of Clavien grade 1-2 perioperative complications at 90-d evaluation.
Description
Comparison between open and robotic arms.
Time Frame
90 days
Title
Incidence of Clavien grade 1-2 perioperative complications at 180-d evaluation.
Description
Comparison between open and robotic arms.
Time Frame
180 days
Title
Incidence of patients requiring readmission.
Description
Comparison between open and robotic arms.
Time Frame
90 days
Title
Cost analysis.
Description
Comparison between open and robotic arms.
Time Frame
30 days
Other Pre-specified Outcome Measures:
Title
Assessment of quality of life at 6-mo follow-up with self-administered EORTC QLQ-BLM30 questionnaire
Description
Comparison between open and robotic arms.
Time Frame
6 months
Title
Assessment of quality of life at 6-mo follow-up with self-administered EORTC QLQ-C30 questionnaire
Description
Comparison between open and robotic arms.
Time Frame
6 months
Title
Assessment of quality of life at 12-mo follow-up with self-administered EORTC QLQ-BLM30 questionnaire
Description
Comparison between open and robotic arms.
Time Frame
12 months
Title
Assessment of quality of life at 12-mo follow-up with self-administered EORTC QLQ-C30 questionnaire
Description
Comparison between open and robotic arms.
Time Frame
12 months
Title
Assessment of quality of life at 24-mo follow-up with self-administered EORTC QLQ-BLM30 questionnaire
Description
Comparison between open and robotic arms.
Time Frame
24 months
Title
Assessment of quality of life at 24-mo follow-up with self-administered EORTC QLQ-C30 questionnaire
Description
Comparison between open and robotic arms.
Time Frame
24 months
Title
Disease free survival
Description
Comparison between open and robitic arms
Time Frame
24 months
Title
Cancer specific survival
Description
Comparison between open and robitic arms
Time Frame
24 months
Title
Overall survival
Description
Comparison between open and robitic arms
Time Frame
24 months
Title
Assessment of urinary continence with pad test.
Description
Comparison between open and robotic arms
Time Frame
12 months
Title
Assessment of urinary continence with pad test.
Description
Comparison between open and robotic arms
Time Frame
24 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with muscle invasive high grade urothelial carcinoma (and variant histologies) of the bladder or high grade non muscle invasive BCG recurrent/refractory disease. Exclusion Criteria: Cystectomy without curative intent (palliative, salvage). Patients unfit for robotic cystectomy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giuseppe Simone, PhD
Organizational Affiliation
"Regina Elena" National Cancer Institute, Dept of Urology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Regina Elena NCI
City
Rome
State/Province
Lazio
ZIP/Postal Code
00144
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33712389
Citation
Mastroianni R, Tuderti G, Anceschi U, Bove AM, Brassetti A, Ferriero M, Zampa A, Giannarelli D, Guaglianone S, Gallucci M, Simone G. Comparison of Patient-reported Health-related Quality of Life Between Open Radical Cystectomy and Robot-assisted Radical Cystectomy with Intracorporeal Urinary Diversion: Interim Analysis of a Randomised Controlled Trial. Eur Urol Focus. 2022 Mar;8(2):465-471. doi: 10.1016/j.euf.2021.03.002. Epub 2021 Mar 10.
Results Reference
derived

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Open Versus Robot Assisted Radical Cystectomy With Totally Intracorporeal Urinary Diversion.

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